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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 505701Generated: November 2, 2026

Methanol → Methyl 5-oxo-5,6,7,8-tetrahydronaphthalene-2-carboxylate

https://huagongshe.com/reaction/505701

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant5-Oxo-5,6,7,8-tetrahydronaphthalene-2-carboxylic acidHCID 2818493—
SolventHydrochloric AcidHCID 313—
ProductMethyl 5-oxo-5,6,7,8-tetrahydronaphthalene-2-carboxylateHCID 1530911686%

Reaction Steps

A solution of 5-oxo-5,6,7,8-tetrahydronaphthalene-2-carboxylic acid (5.14 g, 27.0 mmol) (Peakdale Molecular) in 4N hydrochloric acid in methanol was heated to reflux for eighteen hours. The solution was returned to ambient temperature and concentrated in vacuo. The residue was diluted with ethyl acetate and washed with saturated sodium bicarbonate solution and saturated sodium chloride and dried over magnesium sulfate. Filtration followed by concentration in vacuo provided methyl 5-oxo-5,6,7,8-tetrahydronaphthalene-2-carboxylate as a brown solid (4.76 g, 86% yield). Reversed-phase HPLC on 4.6×50 mm C-18 column, tR=1.90 minutes (10 to 90% acetonitrile/water over 4 minutes at 4 mL/minute with detection 254 nm, at 20° C.); 1H NMR (400 MHz, DMSO-d6) δ ppm 1.99-2.08 (m, 2H), 2.58-2.66 (m, 2H), 2.99 (t, J=6.04 Hz, 2H), 3.85 (s, 3H), 7.83-7.87 (m, 1H), 7.91 (d, J=0.81 Hz, 1H), 7.92-7.97 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07781428B2
Source datasetuspto-grants-2010_08
ORD IDord-9fac2d9edb0545da8095f7947b4aa171
Source noteuspto-grants-2010_08